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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	October 29, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **8151 - 8175** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
51805	coenzyme Q3, methyltransferase	COQ3	Homo sapiens (human)
27235	coenzyme Q2, polyprenyltransferase	COQ2	Homo sapiens (human)	coenzyme Q10 deficiency disease glucose intolerance multiple system atrophy nephrotic syndrome primary coenzyme Q10 deficiency 1
80219	coenzyme Q10B	COQ10B	Homo sapiens (human)
10920	COP9 signalosome subunit 8	COPS8	Homo sapiens (human)
51138	COP9 signalosome subunit 4	COPS4	Homo sapiens (human)
9318	COP9 signalosome subunit 2	COPS2	Homo sapiens (human)
22820	COPI coat complex subunit gamma 1	COPG1	Homo sapiens (human)
9276	COPI coat complex subunit beta 2	COPB2	Homo sapiens (human)
1314	COPI coat complex subunit alpha	COPA	Homo sapiens (human)
64326	COP1 E3 ubiquitin ligase	COP1	Homo sapiens (human)
1312	catechol-O-methyltransferase	COMT	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Balo concentric sclerosis Clostridium difficile colitis Cockayne syndrome DiGeorge syndrome Dowling-Degos disease Down syndrome Gilles de la Tourette syndrome Graves' disease Hirschsprung's disease Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kleine-Levin syndrome Langerhans-cell histiocytosis Laron syndrome Lewy body dementia Lynch syndrome Meckel syndrome Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Parkinsonism Pick's disease Reye syndrome Wernicke-Korsakoff syndrome Wolfram syndrome 1 Wolfram syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne acquired immunodeficiency syndrome acrodermatitis acute myocardial infarction adenocarcinoma adenoma adrenal gland cancer adrenoleukodystrophy adult lymphoma agnosia alcohol dependence alcohol use disorder alexia allergic asthma alternating hemiplegia of childhood amnestic disorder amphetamine abuse androgen insensitivity syndrome anencephaly anorexia nervosa antisocial personality disorder anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autonomic neuropathy autosomal dominant polycystic kidney disease avoidant personality disorder bipolar disorder bladder carcinoma borderline personality disorder breast cancer breast carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma bulimia nervosa bullous congenital ichthyosiform erythroderma cancer cannabis abuse cannabis dependence cardiovascular system disease carpal tunnel syndrome cataract central nervous system disease central nervous system lymphoma central nervous system origin vertigo central sleep apnea cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood disintegrative disease childhood kidney cell carcinoma childhood lymphoma choanal atresia cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma chromosome 17p13.1 deletion syndrome chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma cleft palate clubfoot cocaine abuse cocaine dependence cognitive disorder collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus conduct disorder congenital diarrhea 5 with tufting enteropathy congenital hypothyroidism congenital ptosis conversion disorder corneal neovascularization coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma critical illness polyneuropathy cryptorchidism degenerative disc disease delusional disorder dementia dental caries dental fluorosis dentin caries depressive disorder desquamative interstitial pneumonia diabetes mellitus diabetic ketoacidosis diarrhea disease of mental health dissociative disorder distal myopathy double outlet right ventricle drug dependence drug psychosis duodenum cancer dyslexia dysthymic disorder dystonia eating disorder eclampsia embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis epilepsy episodic kinesigenic dyskinesia 1 episodic kinesigenic dyskinesia 2 esophagitis esophagus squamous cell carcinoma essential hypertension eumycotic mycetoma female breast carcinoma fibrodysplasia ossificans progressiva fibromyalgia gallbladder disease gastroesophageal reflux disease generalized anxiety disorder glaucoma glucose intolerance granular cell carcinoma head and neck squamous cell carcinoma heart cancer heart disease hepatitis C hepatocellular carcinoma heroin dependence herpes simplex holoprosencephaly 1 holoprosencephaly human immunodeficiency virus infectious disease hydrocephalus hypercalcemia hypertension hypertensive encephalopathy hyperthyroidism hypertropia hypoparathyroidism hypospadias hypothyroidism imperforate anus impulse control disorder inappropriate ADH syndrome inflammatory and toxic neuropathy inguinal hernia intellectual disability intermittent explosive disorder intrinsic asthma irritable bowel syndrome isolated cleft palate kidney cancer kleptomania large intestine cancer late onset Parkinson's disease lateral meningocele syndrome learning disability leiomyoma lingual-facial-buccal dyskinesia lissencephaly liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder male infertility mechanical strabismus melancholic depression meningoencephalitis microcephaly microglandular adenosis microphthalmia migraine without aura migraine mitral valve stenosis mood disorder morphine dependence multiple sclerosis myelitis myelomeningocele myeloproliferative disorder with eosinophilia myocardial infarction myofibroma myositis ossificans myositis myxedema narcissistic personality disorder narcolepsy neonatal abstinence syndrome nephrocalcinosis nervous system disease neuroblastoma neurocirculatory asthenia neurodegenerative disease neuropathy neurotic disorder nicotine dependence nodular prostate non-Hodgkin lymphoma nutmeg liver obesity obsessive-compulsive disorder obsessive-compulsive personality disorder obsolete T-cell lymphoblastic leukemia/lymphoma obsolete constipation obsolete dyspepsia obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus obstructive sleep apnea omphalocele ophthalmoplegia opiate dependence optic atrophy osteoarthritis osteochondritis dissecans osteoporosis otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma panic disorder papillary renal cell carcinoma paranoid schizophrenia parapsoriasis patent ductus arteriosus patent foramen ovale pathological gambling peptic esophagitis peripheral nervous system disease pheochromocytoma phobic disorder phosphorus metabolism disease placental insufficiency polycystic ovary syndrome polyhydramnios polyneuropathy post-traumatic stress disorder pre-eclampsia prediabetes syndrome premature ejaculation premature menopause primary immunodeficiency disease primary ovarian insufficiency progressive pseudorheumatoid arthropathy of childhood prostate cancer prostate carcinoma prostatic adenoma pseudohypoparathyroidism psoriasis psychotic disorder ptosis purpura pustulosis of palm and sole rectal benign neoplasm rectum adenocarcinoma rectum cancer recurrent hypersomnia renal carcinoma renal cell carcinoma renal hypoplasia reticulate acropigmentation of Kitamura reticulosarcoma retrograde amnesia rumination disorder sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder schizotypal personality disorder scoliosis seasonal affective disorder seborrheic dermatitis seborrheic infantile dermatitis seborrheic keratosis secondary Parkinson disease senile degeneration of brain sickle cell anemia silent myocardial infarction small intestine cancer social phobia somatization disorder somatoform disorder spina bifida sporadic breast cancer squamous cell carcinoma stomach cancer stomach carcinoma strabismus subacute delirium substance abuse substance-related disorder systemic lupus erythematosus tethered spinal cord syndrome tetralogy of Fallot thrombocytopenia thrombophilia thyrotoxicosis tibial muscular dystrophy tongue squamous cell carcinoma transient myeloproliferative syndrome tricuspid atresia tubular adenocarcinoma type 2 diabetes mellitus umbilical hernia uremia urinary bladder cancer urinary system benign neoplasm urinary system cancer uterine corpus cancer uterine fibroid varicose veins velocardiofacial syndrome ventricular septal defect vesicoureteral reflux visual epilepsy vitiligo withdrawal disorder xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
1311	cartilage oligomeric matrix protein	COMP	Homo sapiens (human)
100532731	COMMD3-BMI1 readthrough	COMMD3-BMI1	Homo sapiens (human)
23127	collagen beta(1-O)galactosyltransferase 2	COLGALT2 Aliases: KIAA0584 Procollagen galactosyltransferase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome bone osteosarcoma breast cancer cerebral degeneration hepatitis A hepatitis lung benign neoplasm osteoarthritis osteosarcoma
79709	collagen beta(1-O)galactosyltransferase 1	COLGALT1 Aliases: FLJ22329 Hydroxylysine galactosyltransferase Procollagen galactosyltransferase	Homo sapiens (human)	Balo concentric sclerosis Simpson-Golabi-Behmel syndrome type 1 adrenoleukodystrophy bone osteosarcoma brain small vessel disease 3 central nervous system disease cerebral degeneration childhood osteosarcoma epilepsy locked-in syndrome narcolepsy osteosarcoma porencephaly quadriplegia visual epilepsy
81035	collectin subfamily member 12	COLEC12 Aliases: CL-P1 SCARA4 SRCL	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis diabetes mellitus familial periodic paralysis multiple sclerosis myopathy substance abuse substance-related disorder type 2 diabetes mellitus
78989	collectin subfamily member 11	COLEC11 Aliases: CL-11 CL-K1 Collectin K1 MGC3279	Homo sapiens (human)	3MC syndrome 1 3MC syndrome 2 3MC syndrome 3 3MC syndrome Bloch-Sulzberger syndrome Chagas disease Klippel-Feil syndrome acquired immunodeficiency syndrome bacterial infectious disease bacterial sepsis blepharophimosis cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism disseminated intravascular coagulation enterobiasis glomerulonephritis human immunodeficiency virus infectious disease humeroradial synostosis hypertropia hypomelanosis of Ito intellectual disability intestinal schistosomiasis isolated cleft palate kidney disease learning disability mechanical strabismus nephritis nephrosis neurodegenerative disease omphalocele ophthalmoplegia pneumonia ptosis purpura fulminans pyoureter radioulnar synostosis schistosomiasis scoliosis sensorineural hearing loss spina bifida occulta spondylolisthesis strabismus trichinosis trypanosomiasis tuberculosis umbilical hernia urinary schistosomiasis viral infectious disease
10584	collectin subfamily member 10	COLEC10 Aliases: CL-10 CL-L1	Homo sapiens (human)	3MC syndrome 3 3MC syndrome Klippel-Feil syndrome Laron syndrome Richter's syndrome achondroplasia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia allergic asthma asthma basal cell carcinoma blepharophimosis cancer carcinoma chronic lymphocytic leukemia cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism essential thrombocythemia hepatocellular carcinoma humeroradial synostosis intellectual disability isolated cleft palate learning disability liver cancer lymphoblastic lymphoma lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance multiple myeloma myelodysplastic syndrome obsolete lymphoplasmacytic lymphoma omphalocele ptosis radioulnar synostosis scoliosis sebaceous carcinoma sensorineural hearing loss spina bifida occulta spondylolisthesis sweat gland cancer umbilical hernia
1299	collagen type IX alpha 3 chain	COL9A3	Homo sapiens (human)
1298	collagen type IX alpha 2 chain	COL9A2 Aliases: MED	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Dowling-Degos disease Ehlers-Danlos syndrome Laron syndrome Laurin-Sandrow syndrome Osgood-Schlatter's disease Stickler syndrome achondroplasia acrodermatitis adult medulloblastoma allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia alternating hemiplegia of childhood amblyopia arthritis arthropathy asthma astigmatism atrial fibrillation autonomic neuropathy bone disease bone osteosarcoma cancer cardiovascular system disease cartilage disease cataract central nervous system cancer central nervous system disease childhood medulloblastoma childhood osteosarcoma chondrodysplasia punctata chronic kidney disease cleft palate collagen disease connective tissue disease degenerative disc disease depressive disorder dermatitis diabetes mellitus diastrophic dysplasia disease of metabolism dysplastic nevus syndrome dysthymic disorder epithelioid sarcoma essential hypertension eye disease familial hypercholesterolemia familial mediterranean fever familial periodic paralysis gliosarcoma granuloma annulare heart disease hemoglobin H disease high grade glioma hypertension intrinsic asthma isolated cleft palate major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma mevalonic aciduria mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia 2 multiple epiphyseal dysplasia myopathy myopia nervous system disease neurotic disorder obsolete melancholia osteoarthritis osteochondritis dissecans osteochondrodysplasia osteochondrosis osteogenesis imperfecta osteosarcoma pancreatic ductal adenocarcinoma pseudoachondroplasia reticulate acropigmentation of Kitamura retinal detachment rheumatoid arthritis sarcoma sensorineural hearing loss spinal stenosis spindle cell sarcoma strabismic amblyopia thalassemia thoracic aortic aneurysm type 2 diabetes mellitus
1297	collagen type IX alpha 1 chain	COL9A1	Homo sapiens (human)
1296	collagen type VIII alpha 2 chain	COL8A2	Homo sapiens (human)
1295	collagen type VIII alpha 1 chain	COL8A1	Homo sapiens (human)
1294	collagen type VII alpha 1 chain	COL7A1	Homo sapiens (human)
131873	collagen type VI alpha 6 chain	COL6A6	Homo sapiens (human)

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